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Crystal structure of nysgrc enolase target 200555, a putative dipeptide epimerase from francisella philomiragia : complex with L- ala-L-glu and L-ala-D-glu

Analyse Crystal structure of nysgrc enolase target 200555, a putative dipeptide… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3R1Z
Type
protein
Length
730 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Enzyme of enolase superfamily
UniProt
B0TZW0
Ligands
SO4
Pockets
8 · best druggability 0.84

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEnzyme of enolase superfamilyprotein36443% helix, 23% strandB0TZW0
BEnzyme of enolase superfamilyprotein36641% helix, 23% strandB0TZW0

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 6 copies · chains A, B
  • GOL · Glycerol · additive · 4 copies · chains A, B

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

8 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110350.840.8489GOL
21520.530.8021empty
31530.510.7924SO4
41180.490.8021empty
5960.480.8115GOL

Interfaces

1 interface between chains.

  • A–B · 1140 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 modified, 1 d-amino (engineered, D-amino acid).

Compared structures

  • 3R1Z · Crystal structure of NYSGRC enolase target 200555, a putative dipeptide epimerase from… · the same entry in another collection · chain A against A, TM-score 1.00
  • B0TZW0 · AlphaFold monomer V2.0 prediction for L-amino acid-D/L-glu epimerase (B0TZW0) · a predicted model of the same protein · chain A against A, TM-score 0.98

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